Evolution of target organ damage and haemodynamic parameters over 4 years in patients with increased insulin resistance: the LOD-DIABETES prospective observational study

ObjectivesWe prospectively examined the impact of type 2 diabetes compared with metabolic syndrome (MetS) on the development of vascular disease over 4 years as determined by anatomic and functional markers of vascular disease. By comparing the vascular outcomes of the 2 disorders, we seek to determ...

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Veröffentlicht in:BMJ open 2016-06, Vol.6 (6), p.e010400-e010400
Hauptverfasser: Gómez-Marcos, Manuel Ángel, Recio-Rodríguez, José Ignacio, Patino-Alonso, María Carmen, Agudo-Conde, Cristina, Rodríguez-Sanchez, Emiliano, Maderuelo-Fernandez, Jose Angel, Gómez-Sánchez, Leticia, Gomez-Sanchez, Marta, García-Ortiz, Luís
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container_end_page e010400
container_issue 6
container_start_page e010400
container_title BMJ open
container_volume 6
creator Gómez-Marcos, Manuel Ángel
Recio-Rodríguez, José Ignacio
Patino-Alonso, María Carmen
Agudo-Conde, Cristina
Rodríguez-Sanchez, Emiliano
Maderuelo-Fernandez, Jose Angel
Gómez-Sánchez, Leticia
Gomez-Sanchez, Marta
García-Ortiz, Luís
description ObjectivesWe prospectively examined the impact of type 2 diabetes compared with metabolic syndrome (MetS) on the development of vascular disease over 4 years as determined by anatomic and functional markers of vascular disease. By comparing the vascular outcomes of the 2 disorders, we seek to determine the independent effect of elevated glucose levels on vascular disease.Setting2 primary care centres in Salamanca, Spain.ParticipantsWe performed a prospective observational study involving 112 patients (68 with type 2 diabetes and 44 with MetS) who were followed for 4 years.Primary and secondary outcome measuresMeasurements included blood pressure, blood glucose, lipids, smoking, body mass index, waist circumference, Homeostasis Model Assessment Insulin Resistance (HOMA-IR), hs-c-reactive protein and fibrinogen levels. We also evaluated vascular, carotid intima media thickness (IMT), pulse wave velocity (PWV) and ankle/brachial index, heart and renal target organ damage (TOD). The haemodynamic parameters were central (CAIx) and peripheral (PAIx) augmentation indices.ResultsIn year 4, participants with type 2 diabetes had increased IMT thickness. These patients had more plaques and an IMT>0.90 mm. In participants with MetS, we only found an increase in the number of plaques. We found no changes in PWV, CAIx and PAIx. The patients with diabetes had a greater frequency of vascular TOD. There were no differences neither in renal nor cardiac percentage of TOD in the patients with MetS or diabetes mellitus type 2.ConclusionsThis prospective study showed that the evolution of vascular TOD is different in participants with type 2 diabetes compared with those with MetS. While IMT and PWV increased in type 2 diabetes, these were not modified in MetS. The renal and cardiac TOD evolution, as well as the PAIx and CAIx, did not change in either group.Trial registration numberNCT01065155; Results.
doi_str_mv 10.1136/bmjopen-2015-010400
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By comparing the vascular outcomes of the 2 disorders, we seek to determine the independent effect of elevated glucose levels on vascular disease.Setting2 primary care centres in Salamanca, Spain.ParticipantsWe performed a prospective observational study involving 112 patients (68 with type 2 diabetes and 44 with MetS) who were followed for 4 years.Primary and secondary outcome measuresMeasurements included blood pressure, blood glucose, lipids, smoking, body mass index, waist circumference, Homeostasis Model Assessment Insulin Resistance (HOMA-IR), hs-c-reactive protein and fibrinogen levels. We also evaluated vascular, carotid intima media thickness (IMT), pulse wave velocity (PWV) and ankle/brachial index, heart and renal target organ damage (TOD). The haemodynamic parameters were central (CAIx) and peripheral (PAIx) augmentation indices.ResultsIn year 4, participants with type 2 diabetes had increased IMT thickness. These patients had more plaques and an IMT&gt;0.90 mm. In participants with MetS, we only found an increase in the number of plaques. We found no changes in PWV, CAIx and PAIx. The patients with diabetes had a greater frequency of vascular TOD. There were no differences neither in renal nor cardiac percentage of TOD in the patients with MetS or diabetes mellitus type 2.ConclusionsThis prospective study showed that the evolution of vascular TOD is different in participants with type 2 diabetes compared with those with MetS. While IMT and PWV increased in type 2 diabetes, these were not modified in MetS. The renal and cardiac TOD evolution, as well as the PAIx and CAIx, did not change in either group.Trial registration numberNCT01065155; Results.</description><identifier>ISSN: 2044-6055</identifier><identifier>EISSN: 2044-6055</identifier><identifier>DOI: 10.1136/bmjopen-2015-010400</identifier><identifier>PMID: 27251684</identifier><language>eng</language><publisher>England: BMJ Publishing Group LTD</publisher><subject>Aged ; Ankle Brachial Index ; Blood Pressure ; Blood Pressure Determination ; C-Reactive Protein - metabolism ; Cardiology ; Carotid Intima-Media Thickness ; Creatinine ; Diabetes ; Diabetes and Endocrinology ; Diabetes Mellitus, Type 2 - complications ; Diabetes Mellitus, Type 2 - physiopathology ; Female ; Glucose ; Hemodynamics ; Humans ; Hypertension ; Insulin Resistance ; Kidney - physiopathology ; Male ; Metabolic syndrome ; Metabolic Syndrome - complications ; Metabolic Syndrome - physiopathology ; Middle Aged ; Prospective Studies ; Pulse Wave Analysis - methods ; Risk Factors ; Software ; Spain ; Ultrasonic imaging ; Values ; Vascular Diseases - diagnostic imaging ; Vascular Diseases - physiopathology ; Vascular Stiffness ; Veins &amp; arteries</subject><ispartof>BMJ open, 2016-06, Vol.6 (6), p.e010400-e010400</ispartof><rights>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing</rights><rights>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 2016 This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b3170-b88e8ce3452e0f03e29d0c532c051a2b7983b7607397d411df80a2f88f0a2efc3</citedby><cites>FETCH-LOGICAL-b3170-b88e8ce3452e0f03e29d0c532c051a2b7983b7607397d411df80a2f88f0a2efc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://bmjopen.bmj.com/content/6/6/e010400.full.pdf$$EPDF$$P50$$Gbmj$$Hfree_for_read</linktopdf><linktohtml>$$Uhttp://bmjopen.bmj.com/content/6/6/e010400.full$$EHTML$$P50$$Gbmj$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27548,27549,27923,27924,53790,53792,77372,77403</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27251684$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gómez-Marcos, Manuel Ángel</creatorcontrib><creatorcontrib>Recio-Rodríguez, José Ignacio</creatorcontrib><creatorcontrib>Patino-Alonso, María Carmen</creatorcontrib><creatorcontrib>Agudo-Conde, Cristina</creatorcontrib><creatorcontrib>Rodríguez-Sanchez, Emiliano</creatorcontrib><creatorcontrib>Maderuelo-Fernandez, Jose Angel</creatorcontrib><creatorcontrib>Gómez-Sánchez, Leticia</creatorcontrib><creatorcontrib>Gomez-Sanchez, Marta</creatorcontrib><creatorcontrib>García-Ortiz, Luís</creatorcontrib><creatorcontrib>LOD-DIABETES Group</creatorcontrib><creatorcontrib>LOD-DIABETES Group</creatorcontrib><title>Evolution of target organ damage and haemodynamic parameters over 4 years in patients with increased insulin resistance: the LOD-DIABETES prospective observational study</title><title>BMJ open</title><addtitle>BMJ Open</addtitle><description>ObjectivesWe prospectively examined the impact of type 2 diabetes compared with metabolic syndrome (MetS) on the development of vascular disease over 4 years as determined by anatomic and functional markers of vascular disease. By comparing the vascular outcomes of the 2 disorders, we seek to determine the independent effect of elevated glucose levels on vascular disease.Setting2 primary care centres in Salamanca, Spain.ParticipantsWe performed a prospective observational study involving 112 patients (68 with type 2 diabetes and 44 with MetS) who were followed for 4 years.Primary and secondary outcome measuresMeasurements included blood pressure, blood glucose, lipids, smoking, body mass index, waist circumference, Homeostasis Model Assessment Insulin Resistance (HOMA-IR), hs-c-reactive protein and fibrinogen levels. We also evaluated vascular, carotid intima media thickness (IMT), pulse wave velocity (PWV) and ankle/brachial index, heart and renal target organ damage (TOD). The haemodynamic parameters were central (CAIx) and peripheral (PAIx) augmentation indices.ResultsIn year 4, participants with type 2 diabetes had increased IMT thickness. These patients had more plaques and an IMT&gt;0.90 mm. In participants with MetS, we only found an increase in the number of plaques. We found no changes in PWV, CAIx and PAIx. The patients with diabetes had a greater frequency of vascular TOD. There were no differences neither in renal nor cardiac percentage of TOD in the patients with MetS or diabetes mellitus type 2.ConclusionsThis prospective study showed that the evolution of vascular TOD is different in participants with type 2 diabetes compared with those with MetS. While IMT and PWV increased in type 2 diabetes, these were not modified in MetS. The renal and cardiac TOD evolution, as well as the PAIx and CAIx, did not change in either group.Trial registration numberNCT01065155; Results.</description><subject>Aged</subject><subject>Ankle Brachial Index</subject><subject>Blood Pressure</subject><subject>Blood Pressure Determination</subject><subject>C-Reactive Protein - metabolism</subject><subject>Cardiology</subject><subject>Carotid Intima-Media Thickness</subject><subject>Creatinine</subject><subject>Diabetes</subject><subject>Diabetes and Endocrinology</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Diabetes Mellitus, Type 2 - physiopathology</subject><subject>Female</subject><subject>Glucose</subject><subject>Hemodynamics</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Insulin Resistance</subject><subject>Kidney - physiopathology</subject><subject>Male</subject><subject>Metabolic syndrome</subject><subject>Metabolic Syndrome - complications</subject><subject>Metabolic Syndrome - physiopathology</subject><subject>Middle Aged</subject><subject>Prospective Studies</subject><subject>Pulse Wave Analysis - methods</subject><subject>Risk Factors</subject><subject>Software</subject><subject>Spain</subject><subject>Ultrasonic imaging</subject><subject>Values</subject><subject>Vascular Diseases - diagnostic imaging</subject><subject>Vascular Diseases - physiopathology</subject><subject>Vascular Stiffness</subject><subject>Veins &amp; 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Recio-Rodríguez, José Ignacio ; Patino-Alonso, María Carmen ; Agudo-Conde, Cristina ; Rodríguez-Sanchez, Emiliano ; Maderuelo-Fernandez, Jose Angel ; Gómez-Sánchez, Leticia ; Gomez-Sanchez, Marta ; García-Ortiz, Luís</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b3170-b88e8ce3452e0f03e29d0c532c051a2b7983b7607397d411df80a2f88f0a2efc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Aged</topic><topic>Ankle Brachial Index</topic><topic>Blood Pressure</topic><topic>Blood Pressure Determination</topic><topic>C-Reactive Protein - metabolism</topic><topic>Cardiology</topic><topic>Carotid Intima-Media Thickness</topic><topic>Creatinine</topic><topic>Diabetes</topic><topic>Diabetes and Endocrinology</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Diabetes Mellitus, Type 2 - physiopathology</topic><topic>Female</topic><topic>Glucose</topic><topic>Hemodynamics</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Insulin Resistance</topic><topic>Kidney - physiopathology</topic><topic>Male</topic><topic>Metabolic syndrome</topic><topic>Metabolic Syndrome - complications</topic><topic>Metabolic Syndrome - physiopathology</topic><topic>Middle Aged</topic><topic>Prospective Studies</topic><topic>Pulse Wave Analysis - methods</topic><topic>Risk Factors</topic><topic>Software</topic><topic>Spain</topic><topic>Ultrasonic imaging</topic><topic>Values</topic><topic>Vascular Diseases - diagnostic imaging</topic><topic>Vascular Diseases - physiopathology</topic><topic>Vascular Stiffness</topic><topic>Veins &amp; arteries</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gómez-Marcos, Manuel Ángel</creatorcontrib><creatorcontrib>Recio-Rodríguez, José Ignacio</creatorcontrib><creatorcontrib>Patino-Alonso, María Carmen</creatorcontrib><creatorcontrib>Agudo-Conde, Cristina</creatorcontrib><creatorcontrib>Rodríguez-Sanchez, Emiliano</creatorcontrib><creatorcontrib>Maderuelo-Fernandez, Jose Angel</creatorcontrib><creatorcontrib>Gómez-Sánchez, Leticia</creatorcontrib><creatorcontrib>Gomez-Sanchez, Marta</creatorcontrib><creatorcontrib>García-Ortiz, Luís</creatorcontrib><creatorcontrib>LOD-DIABETES Group</creatorcontrib><creatorcontrib>LOD-DIABETES Group</creatorcontrib><collection>BMJ Open Access Journals</collection><collection>BMJ Journals:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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By comparing the vascular outcomes of the 2 disorders, we seek to determine the independent effect of elevated glucose levels on vascular disease.Setting2 primary care centres in Salamanca, Spain.ParticipantsWe performed a prospective observational study involving 112 patients (68 with type 2 diabetes and 44 with MetS) who were followed for 4 years.Primary and secondary outcome measuresMeasurements included blood pressure, blood glucose, lipids, smoking, body mass index, waist circumference, Homeostasis Model Assessment Insulin Resistance (HOMA-IR), hs-c-reactive protein and fibrinogen levels. We also evaluated vascular, carotid intima media thickness (IMT), pulse wave velocity (PWV) and ankle/brachial index, heart and renal target organ damage (TOD). The haemodynamic parameters were central (CAIx) and peripheral (PAIx) augmentation indices.ResultsIn year 4, participants with type 2 diabetes had increased IMT thickness. These patients had more plaques and an IMT&gt;0.90 mm. In participants with MetS, we only found an increase in the number of plaques. We found no changes in PWV, CAIx and PAIx. The patients with diabetes had a greater frequency of vascular TOD. There were no differences neither in renal nor cardiac percentage of TOD in the patients with MetS or diabetes mellitus type 2.ConclusionsThis prospective study showed that the evolution of vascular TOD is different in participants with type 2 diabetes compared with those with MetS. While IMT and PWV increased in type 2 diabetes, these were not modified in MetS. The renal and cardiac TOD evolution, as well as the PAIx and CAIx, did not change in either group.Trial registration numberNCT01065155; Results.</abstract><cop>England</cop><pub>BMJ Publishing Group LTD</pub><pmid>27251684</pmid><doi>10.1136/bmjopen-2015-010400</doi><oa>free_for_read</oa></addata></record>
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source BMJ Open Access Journals; MEDLINE; DOAJ Directory of Open Access Journals; PubMed Central Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Aged
Ankle Brachial Index
Blood Pressure
Blood Pressure Determination
C-Reactive Protein - metabolism
Cardiology
Carotid Intima-Media Thickness
Creatinine
Diabetes
Diabetes and Endocrinology
Diabetes Mellitus, Type 2 - complications
Diabetes Mellitus, Type 2 - physiopathology
Female
Glucose
Hemodynamics
Humans
Hypertension
Insulin Resistance
Kidney - physiopathology
Male
Metabolic syndrome
Metabolic Syndrome - complications
Metabolic Syndrome - physiopathology
Middle Aged
Prospective Studies
Pulse Wave Analysis - methods
Risk Factors
Software
Spain
Ultrasonic imaging
Values
Vascular Diseases - diagnostic imaging
Vascular Diseases - physiopathology
Vascular Stiffness
Veins & arteries
title Evolution of target organ damage and haemodynamic parameters over 4 years in patients with increased insulin resistance: the LOD-DIABETES prospective observational study
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